Cited by 621Wnt/β-catenin signaling in development and cancerSignaling Pathways in DiseaseDevelopmental Biology and Gene Regulation

The DOI matches its Crossref record; 28 of the 28 references it cites were found in a registry or an index.

The TAK1–NLK–MAPK-related pathway antagonizes signalling between β-catenin and transcription factor TCF

Ishitani, Tohru, Ninomiya-Tsuji, Jun, Nagai, Shin-ichi, Nishita, Michiru, Meneghini, Marc, Barker, Nick, Waterman, Marian, Bowerman, Bruce, Clevers, Hans, Shibuya, Hiroshi, Matsumoto, Kunihiro·1999·Nature

Abstract

The Wnt signalling pathway regulates many developmental processes through a complex of beta-catenin and the T-cell factor/lymphoid enhancer factor (TCF/LEF) family of high-mobility-group transcription factors. Wnt stabilizes cytosolic beta-catenin, which then binds to TCF and activates gene transcription. This signalling cascade is conserved in vertebrates, Drosophila and Caenorhabditis elegans. In C. elegans, the proteins MOM-4 and LIT-1 regulate Wnt signalling to polarize responding cells during embryogenesis. MOM-4 and LIT-1 are homologous to TAK1 (a kinase activated by transforming growth factor-beta) mitogen-activated protein-kinase-kinase kinase (MAP3K) and MAP kinase (MAPK)-related NEMO-like kinase (NLK), respectively, in mammalian cells. These results raise the possibility that TAK1 and NLK are also involved in Wnt signalling in mammalian cells. Here we show that TAK1 activation stimulates NLK activity and downregulates transcriptional activation mediated by beta-catenin and TCF. Injection of NLK suppresses the induction of axis duplication by microinjected beta-catenin in Xenopus embryos. NLK phosphorylates TCF/LEF factors and inhibits the interaction of the beta-catenin-TCF complex with DNA. Thus, the TAK1-NLK-MAPK-like pathway negatively regulates the Wnt signalling pathway.

Overview

Integrity signals

Registry

Crossref · 10.1038/21674

Cites

28 of 28 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Verification

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Citations

Cites

Flagged first, then by citations

Show all 28 references

Cited by

Sorted by citations

Items 401–500 of 616

Metadata

Authors
Ishitani, T., Ninomiya-Tsuji, J., Nagai, S.-I., Nishita, M., Meneghini, M., Barker, N., Waterman, M., Bowerman, B., Clevers, H., Shibuya, H., & Matsumoto, K.
Affiliations
  • Nagoya University (JP)
  • National Institute for Basic Biology (JP)
  • University of Oregon (US)
  • University of California, Irvine (US)
  • Japan Science and Technology Agency (JP)
Corresponding author
Matsumoto, Kunihiro
Venue
Nature
Published
1999-06
Volume
399
Issue
6738
Pages
798-802
ISSN
  • 0028-0836 (ISSN-L)
  • 1476-4687
OpenAlex
W1902879109
Cited by
621
References
28
Citations by year
2026: 5 · 2025: 10 · 2024: 14 · 2023: 14 · 2022: 6 · 2021: 22 · 2020: 15 · 2019: 12 · 2018: 17 · 2017: 20 · 2016: 18 · 2015: 22 · 2014: 25 · 2013: 21 · 2012: 33
FWCI
10.53
Type
journal article
Language
en
Open access
closed
Locations
  • Nature (publishedVersion)
  • PubMed (publishedVersion)
  • KNAW research portal (Royal Academy of Art and Sciences (KNAW)) (publishedVersion)
  • Data Archiving and Networked Services (DANS) (submittedVersion)
  • RePEc: Research Papers in Economics (submittedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Wnt/β-catenin signaling in development and cancer
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Signaling Pathways in Disease
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
Keywords
Wnt signaling, β-catenin, TCF/LEF transcription factors, TAK1, Nemo-like kinase, MAP3K, DNA binding inhibition, axis duplication, Xenopus embryo, Caenorhabditis elegans
MeSH terms
MAP Kinase Kinase Kinase 7, Animals, Cytoskeletal Proteins, DNA, Humans, Mutation, Phosphorylation, Protein Binding, Transcription Factors, Transfection, Xenopus, Signal Transduction, Trans-Activators, Caenorhabditis elegans, Protein Serine-Threonine Kinases, Point Mutation, Calcium-Calmodulin-Dependent Protein Kinases, COS Cells, Mitogen-Activated Protein Kinases, MAP Kinase Kinase Kinases, Xenopus Proteins, Intracellular Signaling Peptides and Proteins, beta Catenin, TCF Transcription Factors, Transcription Factor 7-Like 2 Protein

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review